The products obtained in the given reactions are shown below. The number of possible products for $x$ and $y$ are:

An ester $(A)$ with molecular formula $C_9H_{10}O_2$ is reacted with an excess of $CH_3MgBr$. The resulting product is treated with concentrated $H_2SO_4$ to form an olefin $(B)$. Ozonolysis of $(B)$ yields a ketone with the formula $C_8H_8O$. What is the structure of $(A)$?

The product $(X)$ of the reaction is:

What are $\underline{A}, \underline{B}, \underline{C}$ in the following reactions?
$(I)$ $(CH_3 CO_2)_2 Ca \stackrel{\Delta}{\longrightarrow} \underline{A}$
$(II)$ $CH_3 CO_2 H \underset{\text{Red P}}{\stackrel{HI}{\longrightarrow}} \underline{B}$
$(III)$ $2 CH_3 CO_2 H \stackrel{P_4 O_{10}}{\longrightarrow} \underline{C}$
$\underline{A} \quad \underline{B} \quad \underline{C}$

The correct acidity order of the following compounds is:

Which of the following sets is in the correct order regarding the property mentioned against them?

Sets	Property
$I$. $NCCH_2COOH > FCH_2COOH > H_3CCH_2COOH$	Acidity
$II$. $CH_3CH_2CHO > PhCOCH_3 > PhCHO$	Reactivity
$III$. $H_3COCH_2CH_3 < H_3CCH_2CHO < H_3CCH_2CH_2OH$	Boiling points